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J Med Chem. 2009 Apr 9;52(7):2036-42. doi: 10.1021/jm801561h.

Substituted terphenyl compounds as the first class of low molecular weight allosteric inhibitors of the luteinizing hormone receptor.

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1
Division of Medicinal Chemistry, Leiden/Amsterdam Center for Drug Research, Leiden University, RA Leiden, The Netherlands.

Erratum in

  • J Med Chem. 2010 Jan 14;53(1):520.

Abstract

The luteinizing hormone (LH) receptor plays an important role in fertility and certain cancers. The endogenous ligands human chorionic gonadotropin (hCG) and LH bind to the large N terminal domain of the receptor. We recently reported on the first radiolabeled low molecular weight (LMW) agonist for this receptor, [(3)H]Org 43553, which was now used to screen for new LMW ligands. We identified a terphenyl derivative that inhibited [(3)H]Org 43553 binding to the receptor, which led us to synthesize a number of derivatives. The most potent compound of this terphenyl series, 24 (LUF5771), was able to increase the dissociation rate of [(3)H]Org 43553 by 3.3-fold (at 10 muM). In a functional assay, the presence of 24 resulted in a 2- to 3-fold lower potency of both Org 43553 and LH. Thus, the compounds presented in this paper are the first LMW ligands that allosterically inhibit the LH receptor.

PMID:
19296599
DOI:
10.1021/jm801561h
[Indexed for MEDLINE]
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